ClinVar Miner

Submissions for variant NM_032856.5(WDR73):c.288-6dup

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV003067680 SCV003459534 benign not provided 2023-01-01 criteria provided, single submitter clinical testing
PreventionGenetics, part of Exact Sciences RCV004550376 SCV004761318 likely benign WDR73-related disorder 2022-12-18 no assertion criteria provided clinical testing This variant is classified as likely benign based on ACMG/AMP sequence variant interpretation guidelines (Richards et al. 2015 PMID: 25741868, with internal and published modifications).

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